- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05175820
COVID-19 and Working Conditions of Dentists
Working Conditions of Dentists During the New Coronavirus (COVID-19) Era
Study Overview
Detailed Description
Within the scope of the study, patient care protocols in public and private health institutions during and after the pandemic, published on the website of the Turkish Dental Association (http://www.tdb.org.tr/) A survey consisting of 35 open-ended and multiple-choice questions was prepared based on the updated directive titled.
The questions directed to dentists in the prepared questionnaire are distributed as follows:
- Demographic information (6 questions),
- Physical conditions of the unit to be served (5 questions),
- Applications for employees (2 questions),
- Applications for appointment and patient admission (4 questions),
- Study procedure and treatment protocols (10 questions),
- Attitudes towards COVID-19 (8 questions) Existing questionnaire questions were examined by 5 dentists for clarity and finalized.
A pilot study was conducted on a group of 20 dentists before the prepared questionnaire started to work. The reliability of the questionnaire was evaluated by retesting this group of 20 people 10 days later. 20 people included in the pilot study were evaluated within the scope of the study.
Survey questions were shared online. According to the data of the Turkish Dental Association, survey questions were sent to the registered dentists in the chambers.
Before the survey questions appear on the screen, individuals will be informed of the privacy policy for data collection and consent to volunteering is asked. If they answered "no" to the survey, the survey was closed automatically. A second reminder email was sent to those who did not respond to the questionnaire four days later. A reminder e-mail was sent to those who did not respond to the questionnaire, six days after the start date.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
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Istanbul, Turkey
- Istanbul University, Faculty of Dentistry
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
- Undergrafute students who have not graduated from the faculty of dentistry,
- Dentists who are not registered in the Turkish Dental Association
Description
Inclusion Criteria:
- Graduated from a dentistry faculty,
- Continuing or not continuing postgraduate dentistry education (master, specialty, doctorate),
- Working in a practice or outpatient clinic, private or public hospital, private polyclinic or state oral and dental health center or university hospital,
- All dentists registered in dentistry database in Turkey (37 cities)
Exclusion Criteria:
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Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Dentists
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Survey questions were sent through the mailing list of the Turkish Dental Association, where all dentists in Turkey are registered
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Infection prevention
Time Frame: 6 months
|
Questionnaire
|
6 months
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Director: Figen Seymen, Prof., Department of Pedodontics, Faculty of Dentistry, Istanbul University
- Principal Investigator: Yelda Kasimoglu Eldem, Assoc. Prof., Department of Pedodontics, Faculty of Dentistry, Istanbul University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2020/47
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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